Great Lakes Dairy Sheep Symposium - the Department of Animal ...
Great Lakes Dairy Sheep Symposium - the Department of Animal ...
Great Lakes Dairy Sheep Symposium - the Department of Animal ...
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
EPA and DHA in sheep milk is similar to that <strong>of</strong> cows’ milk, with fish oil, and to a greater<br />
extent, rumen-protected fish oil allowing for an increase in <strong>the</strong> omega-3 content <strong>of</strong> sheep milk<br />
(Chikunya et al., 2002; Kitessa et al., 2003). There has also been some success in <strong>the</strong> use <strong>of</strong><br />
marine algae to alter EPA and particularly DHA in growing lambs (Cooper et al., 2004).<br />
The intake <strong>of</strong> cis-9, trans-11 CLA in humans is <strong>of</strong> interest because <strong>of</strong> <strong>the</strong> potential health<br />
benefits it may confer. In particular, <strong>the</strong> anticarcinogenic activity <strong>of</strong> cis-9, trans-11 CLA has<br />
been clearly established with in vitro cell culture systems and in vivo animal models for a wide<br />
range <strong>of</strong> cancer types, with <strong>the</strong> antia<strong>the</strong>rogenic properties also now being established (Bauman et<br />
al., 2005a). The major dietary sources <strong>of</strong> cis-9, trans-11 CLA are foods derived from ruminants,<br />
with about 70% and 25% coming from dairy products and red meat, respectively, with cis-9,<br />
trans-11 CLA representing >90% <strong>of</strong> total CLA found in ruminant products (Parodi, 2003). The<br />
presence <strong>of</strong> cis-9, trans-11 CLA in ruminant milk and meat is related to rumen fermentation and<br />
originates mainly from endogenous syn<strong>the</strong>sis in <strong>the</strong> mammary gland; only a minor portion comes<br />
from production in <strong>the</strong> rumen. The substrate used to form cis-9, trans-11 CLA is vaccenic acid<br />
(trans-11 18:1) produced as an intermediate during rumen biohydrogenation, and <strong>the</strong> enzyme<br />
that catalyzes <strong>the</strong> reaction is Δ 9 -desaturase (Figure 4). Due to <strong>the</strong> precursor:product relationship<br />
between vaccenic acid and cis-9, trans-11 CLA, a close linear relationship has been reported for<br />
<strong>the</strong> milk fat content <strong>of</strong> <strong>the</strong>se fatty acids in dairy cows. This same relationship is shown in Figure<br />
5 for sheep milk fat from our study reported above and a similar relationship was also observed<br />
by Nudda et al. (2005).<br />
Figure 4. Pathways for <strong>the</strong> biosyn<strong>the</strong>sis <strong>of</strong> cis-9, trans-11 conjugated linoleic acid (CLA) in<br />
ruminants. Adapted from Bauman and Lock (2005).<br />
Linolenic acid<br />
cis-9, cis-12, cis-15 18:3<br />
cis-9, trans-11, cis-15 18:3<br />
trans-11, cis-15 18:2<br />
Rumen<br />
Linoleic acid<br />
cis-9, cis-12 18:2<br />
cis-9, trans-11 CLA<br />
trans-11 18:1<br />
18:0<br />
Numerous studies have shown that diet is <strong>the</strong> most significant factor affecting <strong>the</strong> cis-9,<br />
trans-11 CLA content <strong>of</strong> milk fat, and its concentration can be increased several-fold by dietary<br />
means (Lock and Bauman, 2004). The key to increasing milk cis-9, trans-11 CLA is to increase<br />
rumen vaccenic acid output, allowing for increased endogenous syn<strong>the</strong>sis in <strong>the</strong> mammary gland.<br />
One strategy is to increase <strong>the</strong> dietary intake <strong>of</strong> 18-carbon PUFAs by addition <strong>of</strong> seeds or plant<br />
oils high in linoleic and/or linolenic acids (e.g. soybeans or sunflowers) which results in an<br />
76<br />
Tissues<br />
cis-9, trans-11 CLA<br />
D 9 -desaturase<br />
trans-11 18:1